Emerging Perspectives on Dipeptide Repeat Proteins in C9ORF72 ALS/FTD
The most common genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) is a hexanucleotide expansion in the chromosome 9 open reading frame 72 gene (C9ORF72). This hexanucleotide expansion consists of GGGGCC (G4C2) repeats that have been implicated to lead to three ma...
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| Hlavní autoři: | , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
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Frontiers Media S.A.
2021-02-01
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| Edice: | Frontiers in Cellular Neuroscience |
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| On-line přístup: | https://www.frontiersin.org/articles/10.3389/fncel.2021.637548/full |
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